Abstract
A sol-gel- derived carboxyl-functionalized lamellar-type silsesquioxane was prepared to investigate its potential for use as a host material for intercalation reactions with n-alkylamines and alkylene diamines. Upon intercalation of n-alkylamines and alkylene diamines, the interlayer distances increased as shown by X-ray powder diffraction patterns, and IR spectra showed the presence of absorption bands attributable to ν(COO-) and δ(NH3+) modes. The amounts of intercalated n-alkylamines were determined from n-CnH2n+1NH2/-COOH molar ratios which, based on CHN analysis, exhibited values from 0.76 to 0.88; whereas the values determined for the alkylene diamines were 0.83 (NH2C4H8NH2), 0.45 (NH2C8H16NH2) and 0.33 (NH2C12H24NH2). These results show that intercalation of n-alkylamines and alkylene diamines into lamellar-type silsesquioxane bearing carboxyl groups proceeded successfully via acid-base mechanisms.
Original language | English |
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Pages (from-to) | 1090-1093 |
Number of pages | 4 |
Journal | Journal of the Ceramic Society of Japan |
Volume | 124 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2016 Oct |
Keywords
- Acid-base mechanism
- Alkylene diamine
- Intercalation
- Lamellar material
- N-Alkylamine
- Sol-gel process
ASJC Scopus subject areas
- Ceramics and Composites
- Chemistry(all)
- Condensed Matter Physics
- Materials Chemistry